Assay Details
Target Gene Details
Entrez Gene ID: | 2999 |
Gene Name: | granzyme H |
Gene Aliases: |
CCP-X, CGL-2, CSP-C, CTLA1, CTSGL2 |
Location: |
Chr.14:24606480-24609763 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GZMH | NM_001270780.1 | 5 | 689 | NP_001257709.1 |
NM_001270781.1 | 4 | 623 | NP_001257710.1 | |
NM_033423.4 | 5 | 881 | NP_219491.1 | |
XM_011536683.2 | 5 | 937 | XP_011534985.1 | |
AW204493.1 | 1 | 107 | ||
AY232657.1 | 4 | 613 | AAP70247.1 | |
AY232658.1 | 3 | 435 | AAP70248.1 | |
BC027974.1 | 5 | 819 | AAH27974.1 | |
BQ054303.1 | 5 | 881 | ||
CD000418.1 | 5 | 658 | ||
M36118.1 | 5 | 826 | AAA03248.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv510631 | Chr.14:24575977 - 24703105 on Build GRCh38 | Deletion | CTSG GZMB GZMH |
More Information
Additional Information:
For this assay, SNP(s) [rs115493987] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Exonic DGV Variation |